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CAS 1010836-19-7

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2-CARBOXYTHIOPHENE-4-BORONIC ACID PINACOL ESTER

Description:
2-Carboxythiophene-4-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a thiophene ring. This compound typically exhibits properties associated with both boron and thiophene derivatives, such as potential applications in organic electronics, pharmaceuticals, and materials science. The pinacol ester moiety enhances its stability and solubility, making it suitable for various synthetic applications. The carboxylic acid group contributes to its reactivity, allowing for further functionalization and coupling reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, the thiophene ring can impart unique electronic properties, making this compound of interest in the development of organic semiconductors. Overall, 2-carboxythiophene-4-boronic acid pinacol ester is a versatile building block in organic synthesis, with potential applications in advanced materials and medicinal chemistry.
Formula:C11H15BO4S
Synonyms:
  • 2-Thiophenecarboxylic acid, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-thiophene-2-carboxylic acid methyl ester
  • 2-CARBOXYTHIOPHENE-4-BORONIC ACID PINACOL ESTER
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